Hara Satoshi, Sanatani Tama, Tachikawa Natsuo, Yoshimura Yukihiro, Miyata Nobuyuki, Sasaki Hiroaki, Kuroda Risa, Kamikokuryo Chinatsu, Eguchi Tomohiro, Niiyama Shuhei, Kakihana Yasuyuki, Ichinose Hiroshi
School of Life Science and Technology, Tokyo Institute of Technology, Yokohama, Japan.
Division of Infectious Disease, Yokohama Municipal Citizen's Hospital, Yokohama, Kanagawa, Japan.
Heliyon. 2022 May;8(5):e09371. doi: 10.1016/j.heliyon.2022.e09371. Epub 2022 May 4.
Neopterin (NP) is a biomarker for activated cellular immunity and is elevated in diseases including viral and bacterial infections, autoimmune diseases, and cancer. However, the clinical assessment of neopterin has not been used for these disorders because the physiological significance of measuring NP is obscure. It would be important to compare the NP profiles with those of other inflammation markers especially in relatively early phase of patients to reveal the significance of NP measurements in pathological states.
Plasma NP, biopterin, CRP, and IL-6 levels were measured in 46 patients with Coronavirus Disease 2019 (COVID-19) and 23 patients with non-COVID-19 disorders. The correlations between these markers were analyzed in the COVID-19 and non-COVID-19 patients independently.
The NP levels were significantly higher in the COVID-19 patients than in the non-COVID-19 patients, while biopterin, CRP and IL-6 were not changed significantly. The NP levels were found to show a weak negative correlation against the days after onset in the COVID-19 patients ( = -0.348, = 0.0192), suggesting that the elevation of NP would be an early event of viral infection. Correlations between NP and CRP, or between NP and IL-6 in COVID-19 patients were weaker than that between CRP and IL-6.
The elevation of NP levels was supposed to be distinct from those of CRP and IL-6 in relatively early and mild COVID-19 patients. Our data suggest that NP is produced at the early phase of infection by different signaling pathways and/or cells from those of CRP and IL-6. Further study on the signaling pathway to induce NP is expected.
新蝶呤(NP)是活化细胞免疫的生物标志物,在包括病毒和细菌感染、自身免疫性疾病及癌症等疾病中升高。然而,新蝶呤的临床评估尚未用于这些疾病,因为测量NP的生理意义尚不清楚。将NP谱与其他炎症标志物的谱进行比较很重要,特别是在患者相对早期阶段,以揭示NP测量在病理状态下的意义。
对46例2019冠状病毒病(COVID-19)患者和23例非COVID-19疾病患者测定血浆NP、生物蝶呤、CRP和IL-6水平。分别在COVID-19患者和非COVID-19患者中分析这些标志物之间的相关性。
COVID-19患者的NP水平显著高于非COVID-19患者,而生物蝶呤、CRP和IL-6无显著变化。发现COVID-19患者的NP水平与发病后天数呈弱负相关(r = -0.348,P = 0.0192),提示NP升高可能是病毒感染的早期事件。COVID-19患者中NP与CRP之间或NP与IL-6之间的相关性弱于CRP与IL-6之间的相关性。
在相对早期和轻度的COVID-19患者中,NP水平的升高被认为与CRP和IL-6不同。我们的数据表明,NP在感染早期由与CRP和IL-6不同的信号通路和/或细胞产生。期待对诱导NP的信号通路进行进一步研究。